A Triad of Unilateral Renal Dysgenesis with Ipsilateral Seminal Vesical and Ejaculatory Duct Obstruction: An Uncommon Urogenital Congenital Anomaly, Zinner Syndrome—A Case Report

Zinner syndrome is a rare congenital anomaly of the urogenital system resulting from an in utero insult during the first trimester. This entity comprises a triad of unilateral renal agenesis/dysgenesis with ipsilateral seminal vesical and ejaculatory duct obstruction. This combination of urinary and...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Rajani Gorantla, Sameera Allu, Ankamma Rao
Formato: article
Lenguaje:EN
Publicado: Thieme Medical and Scientific Publishers Pvt. Ltd. 2021
Materias:
Acceso en línea:https://doaj.org/article/32c7297f0c54457e81f7fa91ffe4b79b
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:32c7297f0c54457e81f7fa91ffe4b79b
record_format dspace
spelling oai:doaj.org-article:32c7297f0c54457e81f7fa91ffe4b79b2021-11-13T23:32:31ZA Triad of Unilateral Renal Dysgenesis with Ipsilateral Seminal Vesical and Ejaculatory Duct Obstruction: An Uncommon Urogenital Congenital Anomaly, Zinner Syndrome—A Case Report0971-30261998-380810.1055/s-0041-1735503https://doaj.org/article/32c7297f0c54457e81f7fa91ffe4b79b2021-07-01T00:00:00Zhttp://www.thieme-connect.de/DOI/DOI?10.1055/s-0041-1735503https://doaj.org/toc/0971-3026https://doaj.org/toc/1998-3808Zinner syndrome is a rare congenital anomaly of the urogenital system resulting from an in utero insult during the first trimester. This entity comprises a triad of unilateral renal agenesis/dysgenesis with ipsilateral seminal vesical and ejaculatory duct obstruction. This combination of urinary and genital abnormalities occurs because of the closely related embryological origin of these structures from the distal mesonephric (Wolffian) duct. Nearly 200 cases of seminal vesical cysts with ipsilateral renal agenesis have been reported in the literature. The affected person generally presents in early adulthood when the reproductive activity commences. In this report, we present a case of a 22-year-old male with complaints of painful ejaculation.Rajani GorantlaSameera AlluAnkamma RaoThieme Medical and Scientific Publishers Pvt. Ltd.articlezinner syndromeurogenitalmesonephric ductMedical physics. Medical radiology. Nuclear medicineR895-920ENIndian Journal of Radiology and Imaging, Vol 31, Iss 03, Pp 707-709 (2021)
institution DOAJ
collection DOAJ
language EN
topic zinner syndrome
urogenital
mesonephric duct
Medical physics. Medical radiology. Nuclear medicine
R895-920
spellingShingle zinner syndrome
urogenital
mesonephric duct
Medical physics. Medical radiology. Nuclear medicine
R895-920
Rajani Gorantla
Sameera Allu
Ankamma Rao
A Triad of Unilateral Renal Dysgenesis with Ipsilateral Seminal Vesical and Ejaculatory Duct Obstruction: An Uncommon Urogenital Congenital Anomaly, Zinner Syndrome—A Case Report
description Zinner syndrome is a rare congenital anomaly of the urogenital system resulting from an in utero insult during the first trimester. This entity comprises a triad of unilateral renal agenesis/dysgenesis with ipsilateral seminal vesical and ejaculatory duct obstruction. This combination of urinary and genital abnormalities occurs because of the closely related embryological origin of these structures from the distal mesonephric (Wolffian) duct. Nearly 200 cases of seminal vesical cysts with ipsilateral renal agenesis have been reported in the literature. The affected person generally presents in early adulthood when the reproductive activity commences. In this report, we present a case of a 22-year-old male with complaints of painful ejaculation.
format article
author Rajani Gorantla
Sameera Allu
Ankamma Rao
author_facet Rajani Gorantla
Sameera Allu
Ankamma Rao
author_sort Rajani Gorantla
title A Triad of Unilateral Renal Dysgenesis with Ipsilateral Seminal Vesical and Ejaculatory Duct Obstruction: An Uncommon Urogenital Congenital Anomaly, Zinner Syndrome—A Case Report
title_short A Triad of Unilateral Renal Dysgenesis with Ipsilateral Seminal Vesical and Ejaculatory Duct Obstruction: An Uncommon Urogenital Congenital Anomaly, Zinner Syndrome—A Case Report
title_full A Triad of Unilateral Renal Dysgenesis with Ipsilateral Seminal Vesical and Ejaculatory Duct Obstruction: An Uncommon Urogenital Congenital Anomaly, Zinner Syndrome—A Case Report
title_fullStr A Triad of Unilateral Renal Dysgenesis with Ipsilateral Seminal Vesical and Ejaculatory Duct Obstruction: An Uncommon Urogenital Congenital Anomaly, Zinner Syndrome—A Case Report
title_full_unstemmed A Triad of Unilateral Renal Dysgenesis with Ipsilateral Seminal Vesical and Ejaculatory Duct Obstruction: An Uncommon Urogenital Congenital Anomaly, Zinner Syndrome—A Case Report
title_sort triad of unilateral renal dysgenesis with ipsilateral seminal vesical and ejaculatory duct obstruction: an uncommon urogenital congenital anomaly, zinner syndrome—a case report
publisher Thieme Medical and Scientific Publishers Pvt. Ltd.
publishDate 2021
url https://doaj.org/article/32c7297f0c54457e81f7fa91ffe4b79b
work_keys_str_mv AT rajanigorantla atriadofunilateralrenaldysgenesiswithipsilateralseminalvesicalandejaculatoryductobstructionanuncommonurogenitalcongenitalanomalyzinnersyndromeacasereport
AT sameeraallu atriadofunilateralrenaldysgenesiswithipsilateralseminalvesicalandejaculatoryductobstructionanuncommonurogenitalcongenitalanomalyzinnersyndromeacasereport
AT ankammarao atriadofunilateralrenaldysgenesiswithipsilateralseminalvesicalandejaculatoryductobstructionanuncommonurogenitalcongenitalanomalyzinnersyndromeacasereport
AT rajanigorantla triadofunilateralrenaldysgenesiswithipsilateralseminalvesicalandejaculatoryductobstructionanuncommonurogenitalcongenitalanomalyzinnersyndromeacasereport
AT sameeraallu triadofunilateralrenaldysgenesiswithipsilateralseminalvesicalandejaculatoryductobstructionanuncommonurogenitalcongenitalanomalyzinnersyndromeacasereport
AT ankammarao triadofunilateralrenaldysgenesiswithipsilateralseminalvesicalandejaculatoryductobstructionanuncommonurogenitalcongenitalanomalyzinnersyndromeacasereport
_version_ 1718430067183321088